35 Bioengineering Jobs

University: Massachusetts Institute of Technology Country: United States Deadline: Not specified Fields: Chemical Engineering, Biomolecular Engineering, Biotechnology, Protein Engineering, Bioprocess Engineering Are you passionate about advancing the frontiers of biologic therapies and eager to apply your expertise in protein engineering to real-world manufacturing challenges? If so, a postdoctoral opportunity in the Sikes Lab at MIT may be the perfect next step in your research career. About The University Or Research Institute The Massachusetts Institute of Technology (MIT) is one of the world’s premier research universities, renowned for its leadership in science, engineering, and technology. Located in Cambridge, Massachusetts, MIT fosters a collaborative and innovative academic environment where interdisciplinary research thrives. Its Chemical Engineering Department is globally recognized for excellence in both fundamental and applied research, and it offers unparalleled resources, mentorship, and connections to industry and academia. Research Topic and Significance This postdoctoral position centers on bioseparations within the context of manufacturing biologic therapies. Bioseparations are essential for the purification and production of therapeutic proteins and biologics, which are increasingly vital in the treatment of a range of diseases. As the demand for biologic medicines grows, efficient and innovative bioseparation techniques are needed to ensure product quality, safety, and scalability. The research conducted in this project has the potential to make significant contributions to the development of next-generation biologic manufacturing processes, ultimately impacting patient care and the biotechnology industry at large. Project Details Also See PhD in Systems Engineering for Sustainable Energy in Manufacturing at TU Delft Lecturer/Senior Lecturer Positions in Bioengineering at UQ Canada – Graduate Positions in Biomanufacturing at McMaster University Postdoctoral Opportunities in Advanced Materials at KFUPM Postdoctoral Opportunities in Small Molecule Chemical Biology at Yale University’s Institute… The successful candidate will join the laboratory of Dr. Hadley Sikes, whose group is known for its work in biomolecular engineering, applications of redox chemistry, clinical diagnostics, and molecular biotechnology. The project involves hands-on, lab-based experimental work in protein engineering and requires strong quantitative skills in engineering design, particularly in reaction kinetics and transport phenomena. The Sikes Lab provides a dynamic and supportive environment, emphasizing both individual initiative and collaborative teamwork. Candidate Profile Applicants Suited For This Postdoctoral Role Should Possess – A strong background in protein engineering, with demonstrated hands-on, experimental laboratory experience. – Expertise in engineering design, including quantitative analysis of reaction kinetics and transport phenomena. – Excellent collaboration skills and a demonstrated ability to work effectively in a team setting. – A genuine interest in biomolecular engineering, redox chemistry applications, clinical diagnostics, or molecular biotechnology. The ideal candidate will be driven, innovative, and eager to contribute to impactful research in the field of biologic therapy manufacturing. Application Process Interested candidates are encouraged to get in touch with Dr. Hadley Sikes by sending a CV if they believe their skills and interests align with the position. For more information about Dr. Sikes and her research, prospective applicants can visit her profile at: https://cheme.mit.edu/profile/hadley-sikes/ No specific application deadline has been mentioned, so early contact is recommended. Conclusion This is an exceptional opportunity for postdoctoral researchers seeking to advance their careers in bioseparations and biologic therapy manufacturing at one of the world’s leading research institutions. If you are interested in joining a collaborative and innovative team at MIT, do not hesitate to reach out with your CV. For more opportunities like this, be sure to follow similar postings and stay connected with the latest advancements in your field. Want to calculate your PhD admission chances? Try it here: https://phdfinder.com/phd_admission_chance_calculator/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

About Velsera Medicine moves too slow. At Velsera, we are changing that. Velsera was formed in 2023 through the shared vision of Seven Bridges and Pierian, with a mission to accelerate the discovery, development, and delivery of life-changing insights. Velsera provides software and professional services for: AI-powered multimodal data harmonization and analytics for drug discovery and development IVD development, validation, and regulatory approval Clinical NGS interpretation, reporting, and adoption With our headquarters in Boston, MA, we are growing and expanding our teams located in different countries! What will you do? Design, develop and maintain various Bioinformatics solutions for analyzing and managing Biological data as per our best practices and quality standards Collaborate with Product Management and Software Engineers, to build bioinformatics solutions Produce high quality and detailed documentation for all projects Provide consultation and technical solutions to cross functional bioinformatics projects Identify and/or conceive novel approaches to better and more efficiently analyze client and public datasets Participate in defining the high-level application architecture for future roadmap requirements and features Coach other team members by sharing domain and technical knowledge and code reviews Participate in activities such hiring and onboarding Work with cross-functional teams to ensure quality throughout the bioinformatics software and analytical pipelines development lifecycle Ensure compliance with our SDLC process during product development Stay up-to-date on technology to deliver quality at each phase of the product life-cycle. You take leadership in evangelizing technical excellence within the team Requirements What do you bring to the table? Ph.D. degree with 3-5+ years of postdoc or industrial experience or Masters Degree in Bioinformatics, Computer Science, Bioengineering, Computational Biology or related field Excellent programming skills in Python and Shell scripting Experience with Relational database such as PostgreSQL, mySQL or Oracle Experience with version control systems such as GitHub Experience with Linux/UNIX/Mac OS X based systems Experience with high-performance Linux cluster and cloud computing (AWS is preferred) Deep understanding of analytical approaches and tools for genomic data analysis along with familiarity with genomic databases. Candidates with proven expertise in the analysis of NGS data generated on sequencing platforms such as Illumina, Oxford Nanopore, or Thermo will be prioritized Experience with open source bioinformatics tools and publicly available variant databases Ability to manage moderately complex projects and initiatives Exceptionally strong communication, data presentation and visualization skills Personal initiative and ability to work effectively with in a cross functional team Excellent communication skills and ability to learn and work independently when necessary High energy and inquisitive and strong attention to detail Benefits Flexible Work & Time Off - Embrace hybrid work models and enjoy the freedom of unlimited paid time off to support work-life balance Health & Well-being - Access comprehensive group medical and life insurance coverage, along with a 24/7 Employee Assistance Program (EAP) for mental health and wellness support Growth & Learning - Fuel your professional journey with continuous learning and development programs designed to help you upskill and grow Recognition & Rewards - Get recognized for your contributions through structured reward programs and campaigns Engaging & Fun Work Culture - Experience a vibrant workplace with team events, celebrations, and engaging activities that make every workday enjoyable & Many More..

Technical Program Manager I/II Program Management Team/Bioinformatics BU (Full Time Employment) Excelra is looking for highly skilled and motivated members for the Program Management Team with technical experience across multiple domains (AI/ML,NGS/human genetics/statistics, software development, project management, agile methodology) in bioinformatics to join the Bioinformatics team. The successful candidate will be expected to demonstrate the following competencies: 1. Project management as well as program management across different projects in key client accounts. 2. Liaison the relationship between client and Excelra 3. Contribute to efforts to increase operational efficiency among projects. 4. Collaboration with delivery for successful delivery of projects 5. Interact with the technical stakeholders of clients to identify new business opportunities. Qualifications: • PhD with 2-3 years of industrial experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology, or related field. • Strong track record of scRNA-Seq and other Omics (NGS) data analysis and downstream systemic interpretation are must. • Good understanding of current best practices in computational biology data-management (NGS/Transcriptiomics/Microarray/Proteomics/Clinical-trials/Text-mining, etc.). • Expertise in one or more programming/scripting languages such as R, Python, shell-script for complex data analysis. • Experience with Docker and Nextflow. • Familiarity with machine learning is an added advantage. • Experience with Linux environment or cloud computing (AWS/GCP) is a plus. • Experience with Relational database such as Postgres, MySQL, or Oracle, is a plus. • Experience with version control systems such as GitHub, is a plus. • Ability to generate in-silico experimental workflows and in-depth knowledge in proprietary and public biological databases, methods, and tools. • Ability to generate scientific hypothesis along with good scientific/technical communication skills would be preferred. Roles & Responsibilities: The selected candidate will be part of the Excelra’s Bioinformatics group. You will be responsible to work with a team in research data analysis in both prospective and retrospective manner to generate the novel hypothesis. • Work with diverse customers/partners in drug discovery and development • Work with multi-disciplinary team of PhD level scientists • Responsible for day-to-day operational activities of Omics (NGS) related projects • Keeping up to date with relevant scientific and technical developments • present the results and scientific hypotheses to internal and external stake holders • Good communication and analytical skills combined with ability to recognize and implement project plans. • Writing research papers, reports, reviews, and su

Job Description for Intern – IT Support under Wadhwani Innovation Network Job Title : Intern – IT Support Department : Wadhwani Innovation Network Location : New Delhi Duration : 6–8 Months Work Mode : Full-time Internship About Wadhwani Foundation Wadhwani Foundation is a not-for-profit with the primary mission of accelerating economic development in emerging economies through large-scale job creation. The Wadhwani Innovation Network (WIN) is dedicated to driving innovation, translation and entrepreneurship with a prime objective of fast-tracking commercialization of academic research in cutting-edge areas such as biotechnology, bioengineering, synthetic biology, healthtech, artificial intelligence, semiconductors, spacetech, advanced computing, quantum technology, critical minerals and mining through partnerships with various Govt. agencies / academic institutions / incubators across the country. Position Overview We are looking for a motivated and detail-oriented intern to support design, development and management of the online grant management portal within the Wadhwani Innovation Network team. This role offers a unique opportunity to work closely with innovators, mentors, software developer and program team, contributing to the unique grant management process supporting academic research into commercialization. What We’re Looking For Bachelors / Masters in Computer Science Engineering / Information Technology or related fields Excellent communication and stakeholder management skills Strong analytical skills – ability to identify and map relevant data and generation of reports Highly organized, with attention to detail and comfort working in a fast-paced environment. Key Responsibilities Support day-to-day coordination with software developer, mentors, innovators and program team Maintain and update trackers, documentation and program dashboards Working closely with program team and software developer for development of online grant management portal Design and test various modules within the grant management portal for operationalization Help in preparing reports, presentations, and communication for outreach Coordinate with innovators and mentors pertaining to the online grant management portal Assist the program team for any other task under Wadhwani Innovation Network as assigned from time to time. Consolidated Remuneration Rs. 20,000 – Rs. 30,000 per month (based on suitability and experience of the candidate). B. Tech - 3rd and 4th Year

Processing & Omega-3 Extraction Specialist Role Summary: We are looking for a Processing & Omega-3 Extraction Specialist to manage and optimize our cold press extraction unit dedicated to fish oil and fish powder production. The role requires technical expertise in food processing, quality control, and machinery operations to ensure premium-grade Omega-3 oil and by-product output. The specialist will also drive compliance with safety, hygiene, and storage standards aligned with FSSAI or pharma-grade benchmarks. Key Responsibilities: Cold Press Unit Operation & Maintenance Operate and oversee cold press extraction machinery for Omega-3 oil and protein powder processing. Ensure optimal extraction temperature, RPM, and throughput to maintain nutrient value. Monitor and calibrate machinery regularly to avoid product loss or contamination. Raw Material Handling Coordinate with the harvest and logistics team for timely procurement of freshly harvested fish. Guide pre-processing techniques such as gutting, degreasing, cleaning, and sorting. Quality Control & Testing Conduct regular quality checks on oil parameters (e.g., DHA/EPA levels, moisture content, peroxide values). Maintain pH, viscosity, odor, and color benchmarks for every batch. Prepare samples for third-party lab testing or regulatory submissions when required. Packaging & Storage Guide filling, sealing, and labeling of Omega-3 oil capsules or bottles. Implement food-grade or pharma-grade storage practices for oil, powder, and by-products. Ensure compliance with packaging standards for commercial and D2C sale. Waste Management & By-Product Utilization Recommend protocols for safe disposal or repurposing of fish waste (e.g., compost, feed supplement, fish meal). Explore secondary use cases like fertilizer grade slurry, gelatin, or animal feed additives. Documentation & Compliance Maintain process logs, batch-wise records, quality testing data, and compliance reports. Assist in FSSAI, AYUSH, or GMP certifications if applicable. Ensure workplace hygiene, PPE usage, and safety protocols. Qualification: Preferred Education: B.Tech / M.Tech in Food Technology, Food Engineering, Bioprocess Engineering, Biotechnology, or Bioengineering from recognized universities or institutes. Experience Required: 3 to 5 years in food/fish processing industries, edible oil units, nutraceuticals, or pharmaceutical-grade oil extraction plants. Exceptional Freshers Welcome: Recent graduates from premier institutes (e.g., CFTRI, ICT, NIFTEM, IIFPT, IITs, state food tech colleges) with strong project work, internship experience, or research background are encouraged to apply. Preferred Attributes: Familiarity with Omega-3 extraction processes, cold pressing, or centrifugation techniques. Hands-on experience with SS 304/316 food-grade machinery, oil filtration units, or encapsulation processes. Awareness of nutritional labeling, safety data sheets (SDS), and ISO/GMP/FSSAI norms. Passion for innovation in health-focused food products and rural enterprise. Location: Processing Unit at Devodhya Foundation Campus – Balni Mehath, Madhubani, Bihar. Employment Type: Full-time, on-site with operational flexibility, safety gear and accommodation support provided. Application Process: Interested applicants can email their updated resume and brief cover note to: support@devodhya.com +91-7260824499 (Ritika Shrivastava – Sr. Executive, CSR) Job Type: Full-time Pay: From ₹10,000.00 per month Schedule: Day shift Work Location: In person

Processing & Omega-3 Extraction Specialist Role Summary: We are looking for a Processing & Omega-3 Extraction Specialist to manage and optimize our cold press extraction unit dedicated to fish oil and fish powder production. The role requires technical expertise in food processing, quality control, and machinery operations to ensure premium-grade Omega-3 oil and by-product output. The specialist will also drive compliance with safety, hygiene, and storage standards aligned with FSSAI or pharma-grade benchmarks. Key Responsibilities: Cold Press Unit Operation & Maintenance Operate and oversee cold press extraction machinery for Omega-3 oil and protein powder processing. Ensure optimal extraction temperature, RPM, and throughput to maintain nutrient value. Monitor and calibrate machinery regularly to avoid product loss or contamination. Raw Material Handling Coordinate with the harvest and logistics team for timely procurement of freshly harvested fish. Guide pre-processing techniques such as gutting, degreasing, cleaning, and sorting. Quality Control & Testing Conduct regular quality checks on oil parameters (e.g., DHA/EPA levels, moisture content, peroxide values). Maintain pH, viscosity, odor, and color benchmarks for every batch. Prepare samples for third-party lab testing or regulatory submissions when required. Packaging & Storage Guide filling, sealing, and labeling of Omega-3 oil capsules or bottles. Implement food-grade or pharma-grade storage practices for oil, powder, and by-products. Ensure compliance with packaging standards for commercial and D2C sale. Waste Management & By-Product Utilization Recommend protocols for safe disposal or repurposing of fish waste (e.g., compost, feed supplement, fish meal). Explore secondary use cases like fertilizer grade slurry, gelatin, or animal feed additives. Documentation & Compliance Maintain process logs, batch-wise records, quality testing data, and compliance reports. Assist in FSSAI, AYUSH, or GMP certifications if applicable. Ensure workplace hygiene, PPE usage, and safety protocols. Qualification: Preferred Education: B.Tech / M.Tech in Food Technology, Food Engineering, Bioprocess Engineering, Biotechnology, or Bioengineering from recognized universities or institutes. Experience Required: 3 to 5 years in food/fish processing industries, edible oil units, nutraceuticals, or pharmaceutical-grade oil extraction plants. Exceptional Freshers Welcome: Recent graduates from premier institutes (e.g., CFTRI, ICT, NIFTEM, IIFPT, IITs, state food tech colleges) with strong project work, internship experience, or research background are encouraged to apply. Preferred Attributes: Familiarity with Omega-3 extraction processes, cold pressing, or centrifugation techniques. Hands-on experience with SS 304/316 food-grade machinery, oil filtration units, or encapsulation processes. Awareness of nutritional labeling, safety data sheets (SDS), and ISO/GMP/FSSAI norms. Passion for innovation in health-focused food products and rural enterprise. Location: Processing Unit at Devodhya Foundation Campus – Balni Mehath, Madhubani, Bihar. Employment Type: Full-time, on-site with operational flexibility, safety gear and accommodation support provided. Application Process: Interested applicants can email their updated resume and brief cover note to: support@devodhya.com +91-7260824499 (Ritika Shrivastava – Sr. Executive, CSR) Job Type: Full-time Pay: From ₹10,000.00 per month Schedule: Day shift Work Location: In person

Our client collaborates with some of the world’s leading AI research labs to build advanced language models that simulate expert reasoning. We are looking for experienced professionals in Biological Sciences, Bioengineering, Biomedical Engineering, Biochemistry, or Biophysics to join a unique AI training initiative. Position: Life Sciences & Biomedical Experts – AI Trainer Type: Hourly Contract (Remote) Compensation: $45–$75/hour Location: Fully remote & asynchronous Duration: 10–20 hrs/week, 1–2 months (extension possible) Role Overview As an AI Trainer, you will leverage your scientific expertise to help train advanced AI systems. You’ll develop prompts, validate AI-generated outputs, and simulate real-world scenarios to ensure technical accuracy and depth in life sciences and biomedical applications. Key Responsibilities Create high-quality prompts and responses reflecting real-world biological and biomedical workflows Validate AI-generated content for scientific accuracy and reasoning rigor Simulate scenarios across life sciences and biomedical domains Collaborate with AI researchers to improve model performance and domain alignment Ideal Qualifications ✅ Advanced degree (Master’s or PhD) in Biology, Molecular Biology, Biomedical Engineering, Bioengineering, Biochemistry, Biophysics , or related fields ✅ 3+ years of professional or research experience in one or more areas: Biological Sciences: Experimental design, molecular/cellular techniques, bioinformatics Biomedical Engineering: Device design, biosignal processing, clinical systems Biochemistry/Biophysics: Protein structure, enzymology, thermodynamic modeling ✅ Strong analytical skills and scientific writing ability ✅ Ability to review content for depth, rigor, and accuracy Preferred: Postdoctoral or industry experience in life sciences or medtech Familiarity with MATLAB, Simulink, PyMOL, GROMACS, PCR systems, or clinical instrumentation

We are seeking an experienced and driven PhD Scientist in biomedical research and laboratory management, specializing in biopolymer-based drug delivery systems. This is a full-time, on-site role based in Lucknow, within a start-up incubated at a premier CSIR research institute, offering a unique opportunity to work at the interface of cutting-edge science and translational innovation. Key Responsibilities: Research & Development: · Design and lead research on biopolymer-based formulations for drug delivery and therapeutic applications. · Conduct in vitro, ex vivo, and in vivo studies to evaluate product safety, performance, and bioactivity. · Use microscopy, imaging, and material analysis tools to study biopolymer behavior and formulation stability. · Develop, optimize, and validate experimental protocols and analytical methods. · Establish and manage a functional laboratory, including equipment setup, procurement, maintenance, and compliance. · Collaborate with multidisciplinary teams across formulation, engineering, and regulatory domains. · Prepare technical reports, manuscripts, and grant proposals to communicate results and secure funding. · Support IP generation, product strategy, and regulatory documentation. Laboratory Establishment & Management: Establish and maintain a fully functional laboratory environment, including equipment setup, procurement, and calibration. Develop and enforce Standard Operating Procedures (SOPs) to ensure consistent experimental practices. Manage laboratory inventory, budgeting, and compliance with health and safety standards. Train and supervise junior staff and students in laboratory techniques, equipment usage, and research protocols. Qualifications: · PhD in Biomedical Sciences, Pharmaceutical Sciences, Bioengineering, or a related field. · 3–5 years of research and lab management experience, with a strong focus on biopolymers and drug delivery. · Proficiency with analytical and imaging tools · Strong leadership, problem-solving, and communication skills. · CSIR-UGC NET qualified candidates will be preferred To apply, send your CV, one-page description of your latest research project, and names and contact information of two References to cellurebiosciences@gmail.com Job Type: Full-time Pay: ₹40,000.00 - ₹50,000.00 per month Ability to commute/relocate: Lucknow, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Required) Education: Doctorate (Required) Experience: Biopolymers: 1 year (Preferred) Work Location: In person Application Deadline: 10/08/2025

R&D Intern – Biomaterials, Mycelium Leather (Unpaid Internship) Location: Remote (with potential on-site requirements) Duration: 3 months Company: MyRei Stipend: Unpaid (Potential for future paid role based on contribution) About MyRei At MyRei , we are developing sustainable, biodegradable, and innovative materials using mycelium and bio-based binders to disrupt the synthetic leather. We are currently in early-stage R&D, prototyping material behavior, and exploring the biofabrication ecosystem to create eco-conscious alternatives for tomorrow. What You'll Work On As a Research & Development Intern , you'll contribute to: Studying research papers and patents on mycelium, algae binders, and bio-inks Reverse-engineering published methods to identify new directions Brainstorming new composite formulations for flexible bio-materials Building detailed mind maps and idea trees from technical literature Supporting our bio-incubation initiatives (possible offline involvement later) Exploring biodegradable alternatives and future design directions for bio-leather Who We’re Looking For Background in Biotechnology / Microbiology / Bioengineering / Material Science Strong interest in biofabrication, biopolymers, or biomaterials Passionate about sustainable alternatives and open to deep research Willingness to work independently and adapt in a dynamic early-stage setup Ideally, hands-on lab experience with fungi or biomaterial cultures is a strong plus Internship Highlights Unpaid role with the potential to transition to a core team or technical R&D head based on contribution Learn startup-level R&D planning, mind mapping, and literature deep dives Remote-first with potential in-person lab work if accepted by any bio incubator All offline expenses (travel, stay, etc.) are self-funded initially If incubated and funded, opportunity to become part of the first technical team Legal & Confidentiality All selected interns must sign an NDA & Confidentiality Agreement to ensure protection of ideas and IP during the research phase. Your ideas and contributions will be documented, credited, and ethically protected. Why Join Us This is not just an internship, it’s a calling for thinkers, tinkerers, researchers, and sustainability enthusiasts who wish to be part of a revolutionary material science startup from the ground up. To Apply: Send a brief note on your interest, background, and any previous relevant experience via DM or email to shaik0abdul0hafeez@gmail.com . Include any research projects or papers you’ve worked on.

Project Development of Microbiome-based Therapeutic Products for Commercialization Profile Jivanu Therapeutics Pvt. Ltd is looking for an accomplished and highly motivated Senior Research Scientist to join our R&D team in Bengaluru, Karnataka. This role offers a unique opportunity to contribute to cutting-edge biotechnology research in a rapidly growing and innovation-driven microbiome-based organization. The ideal candidate will have a strong scientific background, hands-on research experience in a biotech or life sciences domain, expertise in the field of microbiome, and a track record of impactful contributions from premier global institutions. Key Responsibilities Design, lead, and execute high-impact projects focused on product development through bacterial consortia isolation, individual strain isolation, and strain engineering. Experience working with stool samples is preferred. Analyze and interpret complex datasets; ensure high-quality documentation and reproducibility. Drive innovation by identifying and implementing advanced technologies, methodologies, or experimental strategies. Collaborate closely with cross-functional teams including bioinformatics, analytical sciences, and product development. Mentor junior researchers and contribute to a culture of scientific excellence. Present research findings to internal and external stakeholders; contribute to publications, patents, and scientific conferences. Assist with regulatory documentation, grant applications, and technology transfer initiatives. Why Join Us: Be part of a forward-thinking biotech company shaping the future of science and healthcare from Indias innovation hub. Work alongside internationally trained experts in a collaborative and research-driven environment. Access to modern infrastructure, cutting-edge tools, and a vibrant scientific community. Competitive salary, performance incentives, relocation support (if applicable), and career growth opportunities. Industry: Biotechnology Experience Level Senior Qualification Ph.D. in Microbiology, Biotechnology, Molecular Biology, Biochemistry, Bioengineering, or related field. Experience 3 or more years of relevant postdoctoral or industry experience, ideally with exposure to translational or applied research in the field of microbiome. Proven research excellence demonstrated through peer-reviewed publications, patents, or technology development. Strong hands-on expertise in microbiome techniques. Experience managing or leading scientific projects from concept to execution. Excellent communication and organizational skills. Preferred: Prior experience in consortia building, bacterial isolation, and microbiome therapies. Education or work experience at leading international institutions. Experience working in cross-border or multicultural teams. Familiarity with IP generation, regulatory pathways, or translational research pipelines. To Apply: Please submit your CV, a brief statement of research interests, and contact information for 23 professional references.

Nano Micro is a technology startup recognized globally for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These methods enable high-yield, cost-effective production across diverse industries and applications. Meeting purification needs from laboratory to manufacturing scale in both small molecule pharmaceuticals and biopharmaceuticals requires ongoing integration of advancements in chromatography and resin technology, as well as adept management of continually evolving business and scientific challenges. Nano Micro swiftly established itself as an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has since introduced its own brand internationally, with a strategic focus on India, where it has made considerable market advances and successfully expanded operations within major accounts. Now is the perfect time to build a larger team dedicated to increasing market share by penetrating and ramping up volumes within all areas of biopharmaceutical purification. Nano Micro welcomes candidates from a broad range of disciplines, including sales, business development, and scientific research mainly focusing on application support and scaling up in the biopharmaceutical space. At Nano Micro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. The workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity. Nano Micro prioritizes employee growth by supporting professional development and skill enhancement, providing opportunities throughout the organization and actively encouraging staff to engage in new experiences beyond conventional roles. Nano Micro is currently looking for motivated life science scientists to join their India Field Applications Scientist team focused on Biopharmaceuticals. The ideal candidate should be outgoing, confident, and possess strong communication and presentation skills. The candidate should be able to work independently and as part of an energetic sales team that supports research in life sciences, instrumentation, protein purification, separation devices, molecular synthesis, and Organic slime-resistant nano-filtration solutions. The team provides scientific expertise to researchers, labs, and manufacturing sites across India, prioritizing customer needs with their Chromatography Resin portfolio. The primary responsibilities include delivering field-based and remote scientific engagement with customers, developing expertise with protein filtration and purification instruments, and effectively communicating customer feedback to support innovation and market demands. Qualifications for this position include a Masters or PhD in Chemistry, Immunology, Bioengineering, or related field, with Field Application Scientist experience strongly preferred. Candidates should have 5+ years of experience in advanced academic or industry settings, with experience in applications such as vaccines, insulin, plasma proteins, mAbs, oligonucleosides, immunomodulators, GLP-1 peptides, etc. Strong written, verbal, public speaking, interpersonal, and organizational skills are essential, and candidates should be willing to travel 40-60% within the country. To apply, send your resume to srinivas@nanomicrotech.com.,

Nano Micro is a technology startup recognized globally for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These methods enable high-yield, cost-effective production across diverse industries and applications. Meeting purification needs from laboratory to manufacturing scale in both small molecule pharmaceuticals and biopharmaceuticals requires ongoing integration of advancements in chromatography and resin technology, as well as adept management of continually evolving business and scientific challenges. We deliver comprehensive purification solutions for both small molecule and biopharmaceutical sectors, including: · Small molecule therapeutics · Antibody and protein therapeutics · Peptide therapeutics · Oligonucleotide therapeutics · Vaccine discovery and development · Plasma proteins, among others Nano Micro swiftly established itself as an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has since introduced its own brand internationally, with a strategic focus on India, where it has made considerable market advances and successfully expanded operations within major accounts. This is perfect time a larger team dedicated to increasing market share by penetrating and ramp up volumes within all areas of biopharmaceutical purification. Opportunities at Nano Micro Nano Micro welcomes candidates from a broad range of disciplines, including sales, business development, and scientific research mainly focusing on application support and scaling up in biopharmaceutical space. Commitment to Continuous Improvement At Nano Micro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. Collaborative Environment Our workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity. Professional Development Nano Micro prioritizes employee growth by supporting professional development and skill enhancement and provides opportunities throughout the organization. We recognize that learning from setbacks is intrinsic to progress and actively encourage staff to engage in new experiences beyond conventional roles. At Nano Micro, business growth and career development are aligned as employees work to deliver effective resin solutions in all application areas. The company offers competitive pay, performance-based bonuses, and comprehensive benefits in line with startup industry standards. Application Scientists (Multi Location) We are looking for a motivated life science scientists to join our India Field Applications Scientist team focused on Biopharmaceuticals. The ideal candidate is outgoing, confident, and has strong communication and presentation skills. You should be able to work independently and as part of an energetic sales team that supports research in life sciences, and instrumentation – such as protein purification, and separation devices, molecular synthesis, and Organic slime resistant nano filtration solutions. Our team provides scientific expertise to researchers, labs, and manufacturing sites across India, prioritizing customer needs with our Chromatography Resin portfolio. We foster an interactive and supportive nationwide culture. Primary Responsibilities: · Deliver both field-based and remote scientific engagement with customers across pre- and post-sales functions, including tailored 1:1 consultation, product demonstrations, application-focused training, and assay optimization. · Develop in-depth expertise with protein filtration, purification and separation instrument hardware and software while staying current on existing assays, workflows, and emerging applications. · Effectively communicate customer perspectives and feedback to product management, fostering innovation and supporting evolving market demands. Qualifications · Master’s or PhD (preferred) in Chemistry, Immunology, Bioengineering, or related field · Field Application Scientist experience strongly preferred · 5+ years in advanced academic or industry settings · Experience in applications such as vaccines, insulin, plasma proteins, mAbs, oligonucleosides, immunomodulators, GLP-1 peptides, etc. · Strong written, verbal, public speaking, interpersonal, and organizational skills · Willing to travel 40–60% within the country Apply: send your resume to srinivas@nanomicrotech.com

Are you a graduate looking for a challenging yet highly rewarding project? The Extreme Photonics Innovation Centre (EPIC) is a joint UK-India innovation initiative aimed at developing technology for next-generation accelerators using lasers. Funded by the UK Research and Innovation (UKRI), this £4 million centre is jointly established between UK’s Central Laser Facility (CLF) and Tata Institute of Fundamental Research (TIFR). The CLF at the Science and Technology Facilities Council’s Rutherford Appleton Laboratory (RAL), is a world-leader in the next- generation laser technology that can drive compact accelerators yielding bright particle and x-ray beams that, in the near future, can transform imaging capabilities in industry and medicine. TIFR has been pursuing intense laser science over the past two decades and has unraveled many unique features in this field. As part of EPIC Project, we are building a novel microscope for cancer detection. The project is a collaboration between TIFR Hyderabad, TMC Mumbai and STFC UK. It will provide an opportunity to participate in genuine cutting edge research. It will provide valuable research experience in the area of bioengineering, bioimaging and photonics. It will be perfect for someone planning for a career in this area (e.g. someone planning to apply for an industry position or Ph.D. degree in a leading institution). Role Description This is a temporary role for a Project Engineer - Instrumentation at the Tata Institute of Fundamental Research (TIFR) in Hyderabad. The Project Engineer will be responsible for designing, developing, and maintaining instrumentation system of novel microscope used in research. Day-to-day tasks may include conducting laboratory experiments, analyzing data, collaborating with researchers, and providing technical support. This is an on-site role and requires presence in Hyderabad. Essentials Laboratory Skills and ability to conduct research and experiments Has experience in instrument control and data acquisition software Preferably someone with LabView proficiency He/she should have a B.Tech. /M. Tech./M.Sc. degree (or awaiting such a degree). The salary should be commensurate with degree, ability and experience. The end date of the project will be till March 31, 2026

Alien Technology Transfer empowers top-class innovators to transform visionary product concepts into commercial realities. We do this by helping companies with concrete growth ambitions to secure funding for their product development through our innovation consulting expertise. To date, we have raised more than $500 million for our clients - Small and Medium Enterprises (SMEs) - across many domains including agri-tech, artificial intelligence, biotechnology, clean-tech, cyber-security, quantum computing, space, and transport. We are looking for Project Consultants to join our team! Contract Type: Permanent Hybrid Work Modality. You can choose between two options: a) 100% Work From Home OR b) From Monday to Thursday at our Hyderabad Office with Friday Work from Home Project Consultants are in charge of preparing project strategies and drafting our client’s (SMEs) business project proposals to be submitted for the US Federal grant SBIR (Small Business Innovation Research) funding scheme. You have to possess a genuine passion for technology and business, be highly analytical and articulate, have a strong command of English, and a love for writing. You must be a team player, well organized, and also keen to take on responsibility. Key qualities include being able to demonstrate an entrepreneurial mindset and have a high degree of stamina to work within an ambitious and goal-driven environment. In this role, you will be responsible for leading the full range of activities required to conceptualize, prepare, submit, and manage SBIR grant proposals to NIH/NSF. You will be responsible for producing the highest quality scientific documents for funding applications; this includes writing, editing, and proofreading grant proposals. In addition, you will be responsible for supporting our clients as they interface with the Funding Agencies. DUTIES AND RESPONSIBILITIES Project proposal writing: Analyzing business plans and technical documents related to innovative technologies and businesses to be developed within the project; identifying and effectively describing the problems addressed by the innovation and the impact that the innovation will have at USA and global level. Performing technical and business feasibility assessments, identifying and describing the business strategy of the innovative product/ service to be developed within the innovation project. Planning the product development roadmap, including the industrialization activities: preparing the related work plan, risk analysis, GANTT chart, and budgeting. Leading the relationship with the clients and relevant stakeholders involved in the innovative product/ service development process through meetings, calls, and emails. JOB REQUIREMENTS Ph.D. in Life Science (Bioengineering, Biomedical, Biotechnology, Chemistry, Biology, Botany, Zoology, Neurosciences, Biochemistry, Microbiology, Bioinformatics, Computational Biology, etc...); Fluent English; Excellent writing skills; Mid-term stay abroad among past experiences is desirable. Please note: Due to the high volume of candidates we are unfortunately not able to provide individual feedback regarding the outcome of every single application.

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education And Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills And Abilities Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support Benefits We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role: Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education And Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills and Abilities: Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support Benefits We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

ADVERTISEMENT Department of Biological Sciences and Bioengineering Advertisement Number: P.Rect./R&D/2025/122 Applications are invited for the post of Deputy Project Manager under the guidance of Dr. Amitabha Bandyopadhyay, Department of Biological Science and Bioengineering, Indian Institute of Technology, Kanpur. This Post is purely temporary and contractual basis. Designation: Deputy Project Manager Number of positions: One Minimum Qualification: Master’s degree (MA/M.Sc./MBA) with a minimum of 6 years of experience of working in an experimental developmental biology laboratory or other department. Tally & CCC certification & Diploma in office management is necessary. Desirable : Experience in purchase procedures both Import and local purchase, maintaining the stock registers, Vendor management, and bill processing for purchases, Audit and Stock Verification, Administrative and managerial skills, Handling Recruitment Process and Administration, Knowledge of Office Procedures and knowledge of computer i.e., MS Office suite. Duration : Initially for one year and extendable on the basis of performance. Salary : In the range Rs. 23,000 – 2,000 – 59,000/- per month (Consolidated). Last date for receipt of application: 14 th July 2025 , till 5:30 PM. Application Process: Instructions for Candidates : All candidates are requested to duly fill Form 303 (Download link provided below), self-attest all supporting documents, and submit the complete application through the Google Form. Please ensure the following steps are completed: Download and fill Form 303 – https://www.iitk.ac.in/dord/data/303.pdf Self-attest all supporting documents. Fill the Google Form https://forms.gle/Sw7zZKw14adxypRq9 and upload all required documents, including the completed Form 303. Note: Submission of the application is to be done only through the Google Form. No physical copies or email submissions will be accepted. Selection Procedure: The selection will be based on offline interview at IIT Kanpur. Short listed candidate will be informed with an email about the date and time of the interview. Dr. Amitabha Bandyopadhyay Department of Biological Sciences and Bioengineering Indian Institute of Technology Kanpur 208016

ADVERTISEMENT Department of Biological Sciences and Bioengineering Advertisement Number: P.Rect./R&D/2025/109 Applications are invited for the post of Project Multi Skilled Worker (L- 3) under the guidance of Dr. Amitabha Bandyopadhyay, Department of Biological Science and Bioengineering, Indian Institute of Technology, Kanpur. This Post is purely temporary and contractual basis. Designation: Project Multi Skilled Worker (L-3) Number of positions: One Minimum Qualification: 8 th class with a minimum of 15 years of experience of working in an experimental developmental biology laboratory or other department . Desirable : Preference will be given to the candidate having at least 15 years of experience in handling biological laboratory such as autoclaving, media preparation, washing, cleaning and maintenance of machines. Duration : Initially for one year and extendable on the basis of performance. Salary : In the range Rs. 12000-600-36000/- per month (Consolidated). Application Process: Instructions for Candidates : All candidates are requested to duly fill Form 303 (Download link provided below), self-attest all supporting documents, and submit the complete application through the Google Form. Please ensure the following steps are completed: Download and fill Form 303 – https://www.iitk.ac.in/dord/data/303.pdf Self-attest all supporting documents. Fill the Google Form https://forms.gle/Sw7zZKw14adxypRq9 and upload all required documents, including the completed Form 303. Note: Submission of the application is to be done only through the Google Form. No physical copies or email submissions will be accepted. Last date for receipt of application: 14 th July 2025, till 5:30 PM. Selection Procedure: The selection will be based on offline interview at IIT Kanpur. Short listed candidate will be informed with an email about the date and time of the interview. Dr. Amitabha Bandyopadhyay Department of Biological Sciences and Bioengineering Indian Institute of Technology Kanpur 208016

NHS Greater Glasgow and Clyde is one of the largest healthcare systems in the UK employing around 40,000 staff in a wide range of clinical and non-clinical professions and job roles. We deliver acute hospital, primary, community and mental health care services to a population of over 1.15 million and a wider population of 2.2 million when our regional and national services are included. The shift pattern for this post is Monday to Friday. This is a highly rewarding role that provides opportunities for varied and challenging work as the Head of Electronic Engineering for the Medical Devices Unit (MDU), a multi-disciplinary clinical engineering team supporting innovation projects to improve patient diagnosis, treatment and care. MDU staff also provide equipment repair, maintenance and calibration services. The successful candidate will lead a small team of electronic engineers delivering a range of services in support of the wider objectives of the MDU. You will manage the design and development of medical electronic systems to deliver innovative and cost-effective healthcare solutions as part of a wider initiative which focuses on translational research and the development of collaborative projects between NHS Greater Glasgow & Clyde, academia and industry. You will ensure that medical device technical documentation complies with the MDU’s ISO 13485 certified Quality Management System (QMS). You will also manage a calibration service for medical test and diagnostic equipment in compliance with an ISO 55001 certified QMS and will explore service improvement opportunities including UKAS accreditation and service expansion. As the lead for electronic engineering in the Department of Clinical Physics and Bioengineering (DCPB), you will provide expert advice and guidance to clinical and technical staff and will regularly update your technical and regulatory knowledge as it applies to electronic systems with healthcare applications. You will be involved in the strategic development of the MDU and will also take a leading role in the development of its services and systems. You will be a committed, energetic and self-motivated person with good team-working skills and excellent communication and presentation skills. You will be able to demonstrate the following essential attributes: Strong analytical and problem-solving skills; an excellent grasp of state of the art analogue and digital electronics techniques and their application; sound knowledge of electronic design, prototyping and production using industry standard tools; experience of working under Quality Management Systems in a safety critical environment; practical, in-depth experience of a broad range of complex electronic instrumentation; project management of complex electronic design and development projects; and training of technical and scientific staff. Ideally you will have experience of medical equipment and instrumentation and related regulations and standards. You will have an MSc/MEng in Electrical and Electronic Engineering, or other appropriate discipline from a recognised University; or BSc/BEng with profile of knowledge and training equivalent to MSc/MEng. Preferably, you will be a Chartered Engineer, registered with a professional industry body and the Engineering Council. You will normally work 37 hours a week, Monday to Friday. Occasional travel may be required to attend off-site meetings and events. This is a permanent position with a competitive salary and generous holiday entitlement. Informal Contact: Robin Sayer, Head of Mechanical Engineering at Robin.Sayer2@nhs.scot or 0141 211 0091. Details on how to contact the Recruitment Service can be found within the Candidate Information Packs NHS Greater Glasgow and Clyde encourages applications from all sections of the community. We promote a culture of inclusion across the organisation and are proud of the diverse workforce we have. By signing the Armed Forces Covenant, NHSGGC has pledged its commitment to being a Forces Friendly Employer. We support applications from across the Armed Forces Community, recognising military skills, experience and qualifications during the recruitment and selection process. Candidates should provide original and authentic responses to all questions within the application form. The use of artificial intelligence (AI), automated tools, or other third-party assistance to generate, draft, or significantly modify responses is strongly discouraged. By submitting your application, you confirm that all answers are your own work, reflect your personal knowledge, skills and experience, and have not been solely produced or altered by AI or similar technologies. Failure to comply with this requirement may result in your application being withdrawn from the application process. For application portal/log-in issues, please contact Jobtrain support hub in the first instance.

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us . The Data Scientist II will play a crucial role in supporting operational analytics across GPS to ensure products continue to serve most pressing GPS analytics needs, with potential opportunities to build new advanced analytics capabilities such as predictive modelling, simulation, and optimization. The Data Scientist II should have a strong interest in solving business problems, and an eagerness to work on all parts of the analytics value chain, from partnering with IT on data pipelines to operationalizing predictive models in the service of our patients around the world. Roles & Responsibilities Conduct analysis and interpretation of complex data sets to derive meaningful insights and recommendations based on an understanding of GPS priorities, critical issues, and value levers. Collaborate with stakeholders to identify business problems, goals, and KPIs to to design, establish and maintain data pipelines, models and business facing reports and dashboards. Design, develop, and implement a broad array of GPS analytics that solve complex problems in a computationally efficient and statistically valid manner. Identify and implement enhancement and automation of high-value analytics while ensuring they continue to function efficiently. Collaborate proactively with IT teams to develop and enhance data infrastructure, data pipelines, and analytical tools for efficient data collection, processing, and analysis. Prepare reports, dashboards, and presentations to communicate analyses to stakeholders at various levels of the organization. Follow technical best practices in building, maintaining, and enhancing analytics output with scalable solutions, including code version control, pipeline management, deployment, and documentation. Provide training, guidance, and mentorship to junior analysts and team members when required. Work hours that provide sufficient overlap with standard east coast US working hours. Skills and competencies Strong analytical thinking and problem-solving skills with the ability to analyse complex data sets and draw meaningful conclusions. Agile problem-solving ability and desire to learn new things and continuously improve. Proficiency in statistical analysis techniques and methodologies. Strong project management skills and the ability to work independently or as part of a team. Solid understanding of digital analytics tools and platforms and version control. Strong communication skills with the ability to present complex information to non-technical stakeholders in a clear manner. Strong business acumen and strategic thinking, with the ability to translate analytical findings into actionable insights and recommendations. Experience Bachelor's degree in operations research / industrial engineering / supply chain/chemical engineering/bioengineering. Advanced degree (Masters/PHD is a plus). Proven experience (typically 3-5 years) in a hands-on working environment in operation research, supply chain, data analytics and data integration Knowledge and expertise of analytical models such as linear programming, network optimization, goal programming, multiple objective optimizations, decision analysis Markov decision processes Experience working with large datasets, data visualization tools, statistical software packages and platforms (specifically R, Python, advanced SQL, Domino, AWS, GitHub, dbt, Tableau) Experience with simulation software (SIMIO, Arena, etc.) or DES libraries (simmer, simpy) Experience with biotech product development, manufacturing operations, supply chain, and quality control is a significant plus. Experience in the biopharma industry a plus. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About LH2 Holdings LH2Holdings is an AI Operating System to scale digital content brands and creators. We buy or partner with great digital content brands (web platforms, YouTube channels, apps, podcasts, newsletters, etc) and scale them. LH2 is being built by second-time founders, who have scaled tech platforms with hundreds of millions of users in their previous ventures. Our vision is to enable digital creators to scale with the speed and sophistication of large media conglomerates. About The Role We’re seeking a Senior Science Writer who can tell stories that bridge rigorous scientific research and public understanding. You will be responsible for authoring accessible, engaging, and authoritative content across fields like climate science, evolutionary biology, genetics, ecology, conservation, and emerging technologies. This is not just about summarizing studies; it’s about translating them with accuracy, empathy, and impact. If you’re passionate about science and storytelling and love simplifying complexity without diluting meaning, we’d love to meet you. Responsibilities Write 2 high-quality, compelling science articles per day (800–1,200 words each) Break down peer-reviewed research into engaging, accurate, and well-structured content Pitch weekly article ideas drawn from emerging research, science news, and recent academic publications. Interview scientists or researchers when needed and include expert insights in articles Collaborate with editors on tone, structure, and reader engagement strategies Stay current with trends in environmental science, genetics, climate, and sustainability Required Qualifications 3–7 years of professional experience in science journalism, environmental reporting, or academic communication Bachelor’s or Master’s degree in a scientific field (Biology, Environmental Science, Bioengineering, Earth Sciences, or related) Demonstrated ability to write about complex topics in an engaging, accessible way Strong portfolio of science or environmental content Ability to analyze and accurately summarize peer-reviewed research Strong research skills and attention to detail, particularly in interpreting scientific findings Strong editorial instincts with a reader-first mindset Comfortable switching between technical precision and narrative flair Familiarity with academic publishing, citation formats, and scientific terminology Experience working with content management systems and newsroom workflows What We Offer Competitive compensation Remote working options A collaborative editorial team that values clarity, curiosity, and credibility A platform to reach millions of science-curious readers monthly Skills:- Content Writing

As a Consultant, you will be required to address the following: Collaborate in the fulfillment of consulting projects with a special focus on global markets. This will require working closely with other consultants and project managers located in any of our global offices Conduct primary research with healthcare professionals, industry players as well as industry associations, and national agencies Conduct secondary research on large data sets from various data sources Collaborate in the analysis of quantitative and qualitative data for the development of financial models (i.e. eNPV), market models, economic impact models, health-economic models, as well as product adoption and acceptance models Clean, transform, and standardize complex datasets from multiple sources—including EMR, medical and pharmacy claims, and large prescription and healthcare datasets—to ensure consistency and reliability in analysis Design and develop interactive dashboards and reports using Excel and visualization tools (e.g., Power BI, Tableau) to communicate actionable insights to cross-functional team Develop market landscape presentations, market entry strategies, product positioning strategies, and others Work to solve complex business problems Participate in meetings and presentations to clients across the globe Engage in regular global training modules and required Pharmacovigilance training (internal and client-specific) Qualifications A minimum of 2-3 years of demonstrable experience within the healthcare industry in roles related to market insights/analytics, product management, strategy consulting or related roles Education: Master’s degree in Biotechnology, Pharmacy (MPharm), Bioengineering/Biomedical Engineering, Business Administration, or a related field Marketing, management consulting and/or market research, and reimbursement/pricing expertise are a plus Flexibility to work within a multicultural interdisciplinary team across various time zones Fluent in English and preferably speak other foreign languages. Self-motivated with exceptional organizational skills Advanced degree (PhD) a plus

Senior Regulatory Affairs Manager The Senior Regulatory Affairs Manager will be responsible for supporting international regulatory affairs registrations of medical devices across the globe. Job Description This position involves the creation, identification, collection, and entry of regulatory affairs information related to medical devices. The role includes supporting international regulatory submissions, managing country registration requests, and ensuring compliance with global regulatory requirements. The position requires strong organizational skills, effective communication, and the ability to manage multiple tasks efficiently . Essential Responsibilities Create, submit, and maintain product registration requests for submission. Develop, submit, and manage EU MDR, MDSAP, and EN ISO 13485 documents for regulatory compliance. Review and approve submission documents to ensure compliance with regulatory standards. Maintain up-to-date metrics with product registration requests and submission schedules. Track and monitor regulations applicable to medical devices in designated countries. Manage and update internal regulatory databases, including licenses and registration records . Qualifications Educational Background B.S. degree or higher in a technical discipline, preferably in Computer Science, Engineering, Bioengineering, Biology, or Chemistry . Professional Experience 3-7 years of Regulatory Affairs experience in the medical device industry , including international product registrations and new product development. Knowledge and Skills Knowledge: Working knowledge of 510(k) submissions, EU MDR 2017/745, MDSAP, EN ISO 13485, and 21 CFR 820 - Quality System. Skills: Proficient in Microsoft Word, Excel, and PowerPoint. Strong communication skills (oral and written) in English. Excellent project management skills. Ability to manage multiple tasks with strong attention to detail. Self-motivated and comfortable working remotely with international teams. Organized and analytical thinker with problem-solving abilities.  Primary Work Location: Valsad, Gujarat

University: INRAE (French National Research Institute for Agriculture, Food, and Environment) / University of Paris-Saclay Country: France Deadline: 10/06/2025 Fields: Synthetic Biology, Biotechnology, Molecular Biology, Bioengineering, Computational Biology The French National Research Institute for Agriculture, Food, and Environment (INRAE), in partnership with AgroParisTech and the University of Paris-Saclay, invites applications for a PhD position focused on the design of cross- and multi-species genetic circuits. The successful candidate will join the Micalis unit, a collaborative research environment dedicated to advancing bioengineering solutions for agriculture, food, and environmental challenges. This doctoral project aims to develop innovative tools and strategies to facilitate the implementation of genetic circuits in non-model organisms and multi-species communities. The research will support the rapid deployment of synthetic genetic and metabolic circuits in diverse biotechnology applications. Requirements – Master’s degree or Engineering degree in a relevant field – Experience in experimental synthetic biology, including microbiology and molecular/cell biology techniques – Background in programming, bioinformatics, or computational modelling is an asset – Strong communication skills – Willingness to work collaboratively with an interdisciplinary team – Recruitment is subject to validation by the Ministry due to the unit’s status as a Restricted Zone Application Information For further details and to apply, please visit: https://jobs.inrae.fr/en/ot-25811 Remuneration: 2,200€ gross per month Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register

University: INRAE (French National Research Institute for Agriculture, Food, and Environment) / University of Paris-Saclay Country: France Deadline: 10/06/2025 Fields: Synthetic Biology, Biotechnology, Molecular Biology, Bioengineering, Computational Biology The French National Research Institute for Agriculture, Food, and Environment (INRAE), in partnership with AgroParisTech and the University of Paris-Saclay, invites applications for a PhD position focused on the design of cross- and multi-species genetic circuits. The successful candidate will join the Micalis unit, a collaborative research environment dedicated to advancing bioengineering solutions for agriculture, food, and environmental challenges. This doctoral project aims to develop innovative tools and strategies to facilitate the implementation of genetic circuits in non-model organisms and multi-species communities. The research will support the rapid deployment of synthetic genetic and metabolic circuits in diverse biotechnology applications. Requirements – Master’s degree or Engineering degree in a relevant field – Experience in experimental synthetic biology, including microbiology and molecular/cell biology techniques – Background in programming, bioinformatics, or computational modelling is an asset – Strong communication skills – Willingness to work collaboratively with an interdisciplinary team – Recruitment is subject to validation by the Ministry due to the unit’s status as a Restricted Zone Application Information For further details and to apply, please visit: https://jobs.inrae.fr/en/ot-25811 Remuneration: 2,200€ gross per month Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/register Show more Show less